Down syndrome in a population of elderly mentally retarded patients: Genetic-diagnostic survey and implications for medical care
Ninety‐six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic diagnosis, mental functioning and dementia, ophthalmological and audiological abnormalities, and thyroid function. Seventy of the 96 DS patien...
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Published in: | American journal of medical genetics Vol. 85; no. 4; pp. 376 - 384 |
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Abstract | Ninety‐six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic diagnosis, mental functioning and dementia, ophthalmological and audiological abnormalities, and thyroid function. Seventy of the 96 DS patients (73%) were older than 40 years. Only 4.2% were females. Trisomy 21 was found in 86% and mosaic trisomy 21 in 13%. Eighty‐two percent of the patients were moderately or severely mentally retarded, 15% were profoundly retarded, and only 3% mildly retarded. Nineteen percent of the patients had dementia. This number increased to 42% of the patients above the age of 50 years. Epileptic seizures were present in 16.7% of all patients, and in 50% of the patients with dementia. Only 17% of the patients in the present study had normal visual acuity, one‐third had at least moderately reduced vision. This number increased significantly with age: in the age group 50–59 years almost half of the patients had moderate to severe vision loss. Seventy percent of the patients had moderate, severe, or very severe hearing loss, which was undiagnosed before systematic hearing testing was performed. Increased (48%) or decreased (1%) TSH level was found in 49% of the patients examined for thyroid functions. We suggest a regular screening of all adults with DS to diagnose early dementia, epilepsy, hypothyroidism, and early loss of visual acuity and hearing, with special attention to the group of patients who are severely to profoundly mentally retarded and those with advanced age. Cytogenetic studies are necessary to confirm the clinical diagnosis and are essential for genetic counseling purposes. Am. J. Med. Genet. 85:376–384, 1999. © 1999 Wiley‐Liss, Inc. |
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AbstractList | Ninety-six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic diagnosis, mental functioning and dementia, ophthalmological and audiological abnormalities, and thyroid function. Seventy of the 96 DS patients (73%) were older than 40 years. Only 4.2% were females. Trisomy 21 was found in 86% and mosaic trisomy 21 in 13%. Eighty-two percent of the patients were moderately or severely mentally retarded, 15% were profoundly retarded, and only 3% mildly retarded. Nineteen percent of the patients had dementia. This number increased to 42% of the patients above the age of 50 years. Epileptic seizures were present in 16.7% of all patients, and in 50% of the patients with dementia. Only 17% of the patients in the present study had normal visual acuity, one-third had at least moderately reduced vision. This number increased significantly with age: in the age group 50-59 years almost half of the patients had moderate to severe vision loss. Seventy percent of the patients had moderate, severe, or very severe hearing loss, which was undiagnosed before systematic hearing testing was performed. Increased (48%) or decreased (1%) TSH level was found in 49% of the patients examined for thyroid functions. We suggest a regular screening of all adults with DS to diagnose early dementia, epilepsy, hypothyroidism, and early loss of visual acuity and hearing, with special attention to the group of patients who are severely to profoundly mentally retarded and those with advanced age. Cytogenetic studies are necessary to confirm the clinical diagnosis and are essential for genetic counseling purposes. Ninety‐six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic diagnosis, mental functioning and dementia, ophthalmological and audiological abnormalities, and thyroid function. Seventy of the 96 DS patients (73%) were older than 40 years. Only 4.2% were females. Trisomy 21 was found in 86% and mosaic trisomy 21 in 13%. Eighty‐two percent of the patients were moderately or severely mentally retarded, 15% were profoundly retarded, and only 3% mildly retarded. Nineteen percent of the patients had dementia. This number increased to 42% of the patients above the age of 50 years. Epileptic seizures were present in 16.7% of all patients, and in 50% of the patients with dementia. Only 17% of the patients in the present study had normal visual acuity, one‐third had at least moderately reduced vision. This number increased significantly with age: in the age group 50–59 years almost half of the patients had moderate to severe vision loss. Seventy percent of the patients had moderate, severe, or very severe hearing loss, which was undiagnosed before systematic hearing testing was performed. Increased (48%) or decreased (1%) TSH level was found in 49% of the patients examined for thyroid functions. We suggest a regular screening of all adults with DS to diagnose early dementia, epilepsy, hypothyroidism, and early loss of visual acuity and hearing, with special attention to the group of patients who are severely to profoundly mentally retarded and those with advanced age. Cytogenetic studies are necessary to confirm the clinical diagnosis and are essential for genetic counseling purposes. Am. J. Med. Genet. 85:376–384, 1999. © 1999 Wiley‐Liss, Inc. |
Author | Smeets, D.F.C.M. Schoenmaker, A. De Bal, C. Fryns, J.P. Devriendt, K. Verbeek, J.J.M.C. Trommelen, J.C.M. Ropers, H.H. Hamel, B.C.J. Van Buggenhout, G.J.C.M. |
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Keywords | Chromosomal aberration Human Trisomy Prognosis Epilepsy Vision disorder Chromosome G21 Auditory disorder Aneuploidy Down syndrome Hypothyroidism Symptomatology Phenotype Intellectual deficiency Genetics Adult Complication Age Dementia |
Language | English |
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Acta Paediatr 84: 823-827. 1963; 47 1997; 40 1986; 30 1982; 50 1990; 19 1991; 96 1989; 155 1996; 140 1970 1992; 97 1974; 2 1986; 1 1982; 26 1989; 149 1990; 47 1990 1995; 24 1967; 51 1986 1983 1985; 139 1996; 4 1985; 99 1996; 5 1989 1994; 31 1986; 90 1990; 34 1972; 9 1991; 135 1991; 35 1984; 101 1995b.; 39 1981; 25 1997 1995 1994 1992; 35 1992; 36 1962; 54 1991 1995; 4 1987; 17 1989; 28 1995a.; 39 1995; 84 1990; 27 1993; 97 1986; 25 1965 1988; 66 1982; 157 1989; 14 1992; 62 1981; 56 1994; 7 Hoefnagel (BIB32) 1989 Korenberg (BIB41) 1990; 47 (BIB5) 1994 Evenhuis (BIB19) 1992; 36 Gardiner (BIB30) 1967; 51 Caputo (BIB8) 1989; 28 Eissler (BIB16) 1962; 54 Mattei (BIB43) 1981; 56 Buchanan (BIB7) 1990; 19 Friedman (BIB27) 1989; 149 Walsh (BIB62) 1981; 25 Kelly (BIB37) 1996; 5 Thase (BIB56) 1982; 26 Alembik (BIB2) 1996; 4 Evenhuis (BIB24) 1992; 97 Jacobson (BIB33) 1988; 66 Dahle (BIB12) 1986; 90 Stinissen (BIB55) 1970 Fishler (BIB26) 1991; 96 Van Buggenhout (BIB58) 1994; 31 Fuentes (BIB29) 1995; 4 Evers-Kiebooms (BIB25) 1982; 50 Norman (BIB48) 1995 Moss (BIB46) 1991; 35 Aitchinson (BIB1) 1990; 34 Brown (BIB6) 1989; 14 Dinani (BIB13) 1990; 34 Evenhuis (BIB23) 1991 Katz (BIB36) 1994 Dupont (BIB14) 1986; 30 Stinissen (BIB54) 1965 McGrother (BIB45) 1990; 34 Smink (BIB53) 1992; 35 Verpoorten (BIB61) 1995; 24 Pueschel (BIB50) 1995; 84 Mul (BIB47) 1997; 40 Pueschel (BIB49) 1985; 139 Annerén (BIB3) 1992; 62 Evenhuis (BIB21) 1995b; 39 Trommelen (BIB57) 1994; 2 Kinnell (BIB39) 1987; 17 Warburg (BIB63) 1982; 157 Fryns (BIB28) 1986; 25 Evenhuis (BIB18) 1991; 135 Kleczkowska (BIB40) 1990; 27 Shapiro (BIB52) 1985; 99 Schneider (BIB51) 1990 Van Haasen (BIB60) 1986 Edwards (BIB15) 1972; 9 Jones (BIB35) 1997 Janicki (BIB34) 1986; 90 Crandell (BIB10) 1993; 97 Maurizi (BIB44) 1995; 24 Cullen (BIB11) 1963; 47 Harper (BIB31) 1994 Warren (BIB64) 1989; 155 Evenhuis (BIB20) 1995a; 39 Evenhuis (BIB22) 1996; 140 Van der Meulen (BIB59) 1983 Kraijer (BIB42) 1990 Cooper (BIB9) 1984; 101 (BIB4) 1986; 1 Evenhuis (BIB17) 1990; 47 Kennerley Bankes (BIB38) 1974; 2 |
References_xml | – volume: 50 issue: 8 year: 1982 article-title: Diverse parameters bij het syndroom van Down (mongolisme) en andere trisomieën in België publication-title: CBGS Rapport – start-page: 60 year: 1994 end-page: 61 – volume: 4 start-page: 28 issue: Suppl 1 year: 1996 article-title: Anomalies of thyroid function in Down syndrome children publication-title: Eur J Hum Genet – volume: 66 start-page: 457 year: 1988 end-page: 462 article-title: Ophthalmology in mentally retarded adults publication-title: A clinical survey. Acta Ophthalmol – volume: 25 start-page: 243 year: 1981 end-page: 251 article-title: Keratoconus and blindness in 469 institutionalised subjects with Down syndrome and other causes of mental retardation publication-title: J Ment Defic Res – volume: 39 start-page: 19 year: 1995a. end-page: 25 article-title: Medical aspects of ageing in a population with intellectual disability. I. 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Snippet | Ninety‐six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic... Ninety-six adults with Down syndrome (DS) from an institutional setting of 591 mentally retarded were investigated systematically with respect to cytogenetic... |
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SubjectTerms | Adult Biological and medical sciences Chromosome aberrations Cytogenetics Down syndrome Down Syndrome - epidemiology Down Syndrome - genetics Female Hearing - physiology hearing loss Humans Intellectual Disability - etiology Intellectual Disability - pathology Male Medical genetics Medical sciences mental retardation Middle Aged thyroid function Thyroid Gland - metabolism trisomy 21 vision loss Visual Acuity |
Title | Down syndrome in a population of elderly mentally retarded patients: Genetic-diagnostic survey and implications for medical care |
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